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Cell Rep ; 43(6): 114282, 2024 Jun 25.
Article in English | MEDLINE | ID: mdl-38795342

ABSTRACT

The suppressive effect of insulin on food intake has been documented for decades. However, whether insulin signals can encode a certain type of nutrients to regulate nutrient-specific feeding behavior remains elusive. Here, we show that in female Drosophila, a pair of dopaminergic neurons, tritocerebrum 1-dopaminergic neurons (T1-DANs), are directly activated by a protein-intake-induced insulin signal from insulin-producing cells (IPCs). Intriguingly, opto-activating IPCs elicits feeding inhibition for both protein and sugar, while silencing T1-DANs blocks this inhibition only for protein food. Elevating insulin signaling in T1-DANs or opto-activating these neurons is sufficient to mimic protein satiety. Furthermore, this signal is conveyed to local neurons of the protocerebral bridge (PB-LNs) and specifically suppresses protein intake. Therefore, our findings reveal that a brain-derived insulin signal encodes protein satiety and suppresses feeding behavior in a nutrient-specific manner, shedding light on the functional specificity of brain insulin signals in regulating behaviors.


Subject(s)
Brain , Drosophila Proteins , Feeding Behavior , Insulin , Signal Transduction , Animals , Insulin/metabolism , Brain/metabolism , Female , Drosophila Proteins/metabolism , Dopaminergic Neurons/metabolism , Drosophila melanogaster/metabolism , Satiety Response , Nutrients/metabolism
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